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抗精神病药对染铜饮食诱导的少突胶质前体细胞分化的影响。

Differential effects of antipsychotics on the development of rat oligodendrocyte precursor cells exposed to cuprizone.

机构信息

Mental Health Center, Shantou University Medical College, Shantou, People's Republic of China,

出版信息

Eur Arch Psychiatry Clin Neurosci. 2014 Mar;264(2):121-9. doi: 10.1007/s00406-013-0414-3. Epub 2013 Jun 1.

Abstract

Cuprizone (CPZ) is a copper-chelating agent and has been shown to induce white matter damage in mice and rats. The compromised white matter and oligodendrocytes (OLs) respond to some antipsychotics in vivo. However, little is known about the effects of antipsychotics on cultured OLs in the presence of CPZ. The aim of this study was to examine effects of some antipsychotics on developing OLs in the presence of CPZ. Oligodendrocyte progenitor cells (OPCs) were prepared from rat embryos; OLs at different developing stages were labeled with specific antibodies; levels of CNP and MBP proteins in mature OLs were assessed by Western-blot analysis; malondialdehyde (MDA) levels and activity of catalase were evaluated as well for an assessment of oxidative stress and antioxidative status. In immunofluorescent staining, CPZ was shown to inhibit the differentiation of cultured OPCs into O4-positive cells, reduce the maturation of O4-positive cells into CNP- and MBP-positive cells, and decrease levels of CNP and MBP in mature OLs. These inhibitory effects of CPZ were ameliorated by clozapine and quetiapine (QUE), but not by haloperidol and olanzapine. Further experiments were performed to explore the mechanism of the protective effects of QUE. QUE attenuated the decreases in CNP and MBP in CPZ-treated OLs, and blocked the CPZ-induced increase in MDA and decrease in catalase activity in cultured OLs. These results are relevant to the pathophysiology and treatment of schizophrenia considering the aberrant white matter development and evidence suggesting the derangement of the oxidant and antioxidant defense system in some of the patients with schizophrenia.

摘要

铜螯合剂 CPZ 已被证实可诱导小鼠和大鼠的白质损伤。受损的白质和少突胶质细胞 (OLs) 在体内对一些抗精神病药有反应。然而,关于 CPZ 存在时抗精神病药对培养的 OLs 的影响知之甚少。本研究旨在研究 CPZ 存在时一些抗精神病药对发育中的 OLs 的影响。从小鼠胚胎中制备少突胶质前体细胞 (OPC);用特异性抗体标记不同发育阶段的 OLs;通过 Western blot 分析评估成熟 OLs 中 CNP 和 MBP 蛋白的水平;评估丙二醛 (MDA) 水平和过氧化氢酶活性,以评估氧化应激和抗氧化状态。在免疫荧光染色中,CPZ 被证明可抑制培养的 OPC 分化为 O4 阳性细胞,减少 O4 阳性细胞向 CNP 和 MBP 阳性细胞的成熟,并降低成熟 OLs 中 CNP 和 MBP 的水平。CPZ 的这些抑制作用被氯氮平和喹硫平 (QUE) 改善,但不被氟哌啶醇和奥氮平改善。进一步的实验旨在探索 QUE 保护作用的机制。QUE 可减轻 CPZ 处理的 OLs 中 CNP 和 MBP 的减少,并阻断 CPZ 诱导的 OLs 中 MDA 增加和过氧化氢酶活性降低。考虑到精神分裂症患者的白质发育异常和一些患者的氧化应激和抗氧化防御系统紊乱的证据,这些结果与精神分裂症的病理生理学和治疗有关。

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